VIKAMED Patient Monitor - Indonesia BPOM Medical Device Registration
VIKAMED Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420478. The device is manufactured by EDAN INSTRUMENT., INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EDAN INSTRUMENT., INC.Country of Origin
China
Authorized Representative
PT. SEKARGUNA MEDIKAAR Address
JL. Ciputat Raya Nomor 64
Registration Date
Nov 18, 2024
Expiry Date
Nov 17, 2027
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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